透光脉动检测仪研究碱度对絮体形成、破碎及再生的影响

为了解碱度对絮体的形成、破碎及再生过程的影响,采用PDA2000型透光脉动检测仪测定不同碱度下投加硫酸铝时高岭土悬浮液的絮凝指数(FI指数),并以强度因子和再生因子评价絮体的强度和再生能力。结果表明,碱度的高低在很大程度上会影响絮体的形成、破碎及再生过程,所形成絮体的颗粒随碱度的增加而减小。混凝剂投量和碱度高低共同决定了絮体的抗破碎强度,碱度越高,混凝剂投量越大,絮体的强度越高。在电中和作用下形成的絮体在低碱度下经一次破碎后恢复程度接近100%,在网捕卷扫作用下形成的絮体,无论碱度高低,从第2次破碎起,FI指数均以大于10%的幅度逐次下降,絮体不可恢复程度显著增大。     

Temperature‐Sensitive Amorphous Polyurethanes

Abstract

Shape‐memory polymers based on segmental polyurethanes (PUs) were synthesized from 1,3‐butane diol (1,3‐BD), hexamethylene diisocyanate (HDI), and 4,4′‐diphenylmethane diisocyanate (MDI), and characterized in terms of thermomechanical, dynamic mechanical, rheological, and thermal properties. It was found that soft segments (1,3‐BD and HDI) and hard segments (1,3‐BD and MDI) were well phase mixed to give a single glass transition temperature (T _g) that was easily controlled by hard segment content. With the increase in hard segment content, T _g, melt viscosity, rubbery plateau, modulus, relaxation time, and shape recovery increased, and shape fixability for repeated cycles decreased.     

Rotating polarizer,compensator, and analyzer ellipsometry

In this paper we propose theoretically a set of ellipsometric configurations using a rotating polarizer, compensator, and analyzer at a speed ratio of N1ω：N2ω：N3ω. Different ellipsometric configurations can be obtained by giving different integral values to N1, N2, and N3. All configurations are applied to bulk c-Si and GaAs to calculate the real and imaginary parts of the refractive index of the samples. The accuracies of all ellipsometric configurations are investigated in the presence of a hypothetical noise and with small misalignments of the optical elements. Moreover, the uncertainties in the ellipsometric parameters as functions of the uncertainties of the Fourier coefficients are studied. The comparison among different configurations reveals that the rotating compensator–analyzer configuration corresponds to the minimum error in the calculated optical parameters.     

Determination of multiple pesticide residues in teas by gas chromatography with accurate time‐of‐flight mass spectrometry

In this work, gas chromatography tandem with electron ionization and full‐scan high‐resolution mass spectrometry with a time‐of‐flight mass analyzer was evaluated for analyzing pesticide residues in teas. The relevant aspects for mass spectrometry analysis, including the resolution and mass accuracy, acquisition rate, temperature of ion source, were investigated. Under acquisition condition in 2‐GHz extended dynamic range mode, accurate mass spectral library including 184 gas chromatography detectable pesticides was established and retrieval parameters were optimized. The mass spectra were consistent over a wide concentration range (three orders) with good match values to those of NIST (EI‐quadrupole). The methodology was verified by the validation of 184 pesticides in four tea matrices. A wide linear range (1–1000 μg/kg) was obtained for most compounds in four matrices. Limit of detection, limit of quantification, and limit of identification values acquired in this study could satisfy the requirements for maximum residue levels prescribed by the European Community. Recovery studies were performed at three concentrations (10, 50, and 100 μg/kg). Most of the analytes were recovered at an acceptable range of 70–120% with relative standard deviations ≤ 20% in four matrices. The potential extension of qualitative screening scope makes gas chromatography tandem with electron ionization and mass spectrometry with a time‐of‐flight mass analyzer a more powerful tool compared with gas chromatography with tandem mass spectrometry.     

Review of in situ X-ray fluorescence analysis technology in China

In the past two decades, the in situ X-ray fluorescence (XRF) technology has been developed rapidly in China, which is mainly due to the rapid development of China's economy and the great demand for rapid qualitative and quantitative analysis of elements in geological exploration, environmental protection, and industrial process analysis. In this article, the development of in situ XRF analysis technology in China is reviewed from three aspects, namely in situ XRF analyzers, in situ XRF analysis technology, and applications of in situ XRF analysis technology. The in situ XRF analyzers are divided into four generations, and the technical characteristics of each generation of analyzers are discussed from the perspectives of X-ray excitation source, detector, electronic circuit unit, and digital signal processing. The progress of X-ray spectrum analysis, matrix effect correction, and correction of uneven effect and humidity effect is reviewed. The representative applications of XRF analysis technology in geological and mineral survey, environmental pollution investigation, cultural relic identification, and alloy analysis are introduced.     

A Nanometer Aerosol Size Analyzer (nASA) for Rapid Measurement of High-concentration Size Distributions

We have developed a fast-response nanometer aerosol size analyzer (nASA) that is capable of scanning 30 size channels between 3 and 100 nm in a total time of 3 s. The analyzer includes a bipolar charger (Po²¹⁰), an extended-length nanometer differential mobility analyzer (Nano-DMA), and an electrometer (TSI 3068). This combination of components provides particle size spectra at a scan rate of 0.1 s per channel free of uncertainties caused by response-time-induced smearing. The nASA thus offers a fast response for aerosol size distribution measurements in high-concentration conditions and also eliminates the need for applying a de-smearing algorithm to resulting data. In addition, because of its thermodynamically stable means of particle detection, the nASA is useful for applications requiring measurements over a broad range of sample pressures and temperatures. Indeed, experimental transfer functions determined for the extended-length Nano-DMA using the tandem differential mobility analyzer (TDMA) technique indicate the nASA provides good size resolution at pressures as low as 200 Torr. Also, as was demonstrated in tests to characterize the soot emissions from the J85-GE engine of a T-38 aircraft, the broad dynamic concentration range of the nASA makes it particularly suitable for studies of combustion or particle formation processes. Further details of the nASA performance as well as results from calibrations, laboratory tests and field applications are presented below.     

近红外光谱预测汽油辛烷值和辛烷值仪的研制

本文报道了用近红外光谱预测汽油马达法辛烷值,研究法辛烷值和抗爆指数的方法。用多重线性回归和偏最小二乘法回归建立辛烷值的预测模型。基于此模型,首次研制成功光学多道近红外辛烷值仪。     

Well-crystallized zinc oxide quantum dots with narrow size distribution

In this study, pulsed laser ablation, online annealing, and following size classification using a differential mobility analyzer (DMA) were employed to fabricate quantum dots (QDs) of zinc oxide (ZnO). The irregularly shaped ZnO particles were obtained at annealing temperature less than 873 K, which gradually transformed into spherical QDs with increasing the annealing temperature. Finally, ZnO QDs with narrow size distribution having spherical shapes were successfully obtained at temperatures above 1173 K under the DMA classification at a nominal size of 10 nm. TEM observation demonstrated that the ZnO QDs obtained by this process were well-crystallized single crystallites with a wurtzite structure. Further, ZnO QDs with average sizes in the range of 4.8–8.1 nm were successfully fabricated by reducing the specified sizes of DMA. These features of the fabricated ZnO QDs are favorable for investigation of intrinsic quantum size effect in ZnO.     

氟吗啉合成工艺热危险性及动力学研究

氟吗啉是一种新型杀菌剂, 合成工艺热危险性和动力学研究将解决工程问题, 并保障安全生产. 采用差示扫描量热-热重分析仪(DSC-TG)测试主要原料、中间体和产品的热稳定性, 采用反应量热仪(RC1)研究反应热行为, 同时开展反应动力学研究. 研究结果显示, 主要中间体(3,4-二甲氧基苯基)(4-氟苯基)甲酮吸热分解温度为559.3 K, 乙酰吗啉吸热分解温度为478.2 K, 氟吗啉吸热分解温度为638.6 K. 氟吗啉合成反应摩尔放热量为15.44 kJ/mol, 绝热温升ΔT_ad为9.1 K, 本研究合成工艺的热危险性较小. 氟吗啉合成反应动力学方程为：r_A=kc_A^a=8.34×10^-3C_A^0.57, 对主要中间体(3,4-二甲氧基苯基)(4-氟苯基)甲酮的反应级数为0.57 级.